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3.
Pediatr Allergy Immunol ; 35(3): e14096, 2024 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-38425150

RESUMO

BACKGROUND: Allergy to beta-lactam antibiotics (BLA) is frequently suspected in children, but a drug provocation test (DPT) rules it out in over 90% of cases. Direct oral DPT (DODPT), without skin or other previous tests, is increasingly been used to delabel non-immediate BLA reactions. This real-world study aimed to assess the safety and effectiveness of DODPT in children with immediate and non-immediate reactions to BLAs. METHODS: Ambispective registry study in children (<15 years), attended between 2016 and 2023 for suspected BLA allergy in 15 hospitals in Spain that routinely perform DODPT. RESULTS: The study included 2133 patients with generally mild reactions (anaphylaxis 0.7%). Drug provocation test with the implicated BLA was performed in 2014 patients (94.4%): 1854 underwent DODPT (86.9%, including 172 patients with immediate reactions). One hundred forty-five (7.2%) had symptoms associated with DPT, although only four reactions were severe: two episodes of anaphylaxis and two of drug-induced enterocolitis syndrome, which resolved rapidly with treatment. Of the 141 patients with mild reactions in the first DPT, a second DPT was considered in 87 and performed in 57, with 52 tolerating it without symptoms. Finally, BLA allergy was ruled out in 90.9% of the sample, confirmed in 3.4%, and remained unverified, usually due to loss to follow-up, in 5.8%. CONCLUSIONS: Direct oral DPT is a safe, effective procedure even in immediate mild reactions to BLA. Many reactions observed in DPT are doubtful and require confirmation. Severe reactions are exceptional and amenable to treatment. Direct oral DPT can be considered for BLA allergy delabeling in pediatric primary care.


Assuntos
Anafilaxia , Hipersensibilidade a Drogas , Criança , Humanos , beta-Lactamas , Antibacterianos/efeitos adversos , Testes Cutâneos/métodos , Anafilaxia/induzido quimicamente , Hipersensibilidade a Drogas/diagnóstico , Hipersensibilidade a Drogas/epidemiologia , Monobactamas
5.
Laryngoscope ; 134(3): 1437-1444, 2024 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-37497872

RESUMO

OBJECTIVE: Pediatric inferior turbinate hypertrophy (PedTH) is a frequent and often overlooked cause or associated cause of nasal breathing difficulties. This clinical consensus statement (CCS) aims to provide a diagnosis and management framework covering the lack of specific guidelines for this condition and addressing the existing controversies. METHODS: A clinical consensus statement (CCS) was developed by a panel of 20 contributors from 7 different European and North American countries using the modified Delphi method. The aim of the CCS was to offer a multidisciplinary reference framework for the management of PedTH on the basis of shared clinical experience and analysis of the strongest evidence currently available. RESULTS: A systematic literature review following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) criteria was performed. From the initial 96 items identified, 7 articles were selected based on higher-evidence items such as randomized-controlled trials, guidelines, and systematic reviews. A 34-statement survey was developed, and after three rounds of voting, 2 items reached strong consensus, 17 reached consensus or near consensus, and 15 had no consensus. CONCLUSIONS: Until further prospective data are available, our CCS should provide a useful reference for PedTH management. PedTH should be considered a nasal obstructive disease not necessarily related to an adult condition but frequently associated with other nasal or craniofacial disorders. Diagnosis requires clinical examination and endoscopy, whereas rhinomanometry, nasal cytology, and questionnaires have little clinical role. Treatment choice should consider the specific indications and features of the available options, with a preference for less invasive procedures. LEVEL OF EVIDENCE: 5 Laryngoscope, 134:1437-1444, 2024.


Assuntos
Doenças Nasais , Conchas Nasais , Adulto , Humanos , Criança , Conchas Nasais/cirurgia , Endoscopia , Exame Físico , Rinomanometria , Hipertrofia/diagnóstico , Hipertrofia/terapia
6.
Pediatr Pulmonol ; 58(11): 3195-3205, 2023 11.
Artigo em Inglês | MEDLINE | ID: mdl-37589420

RESUMO

INTRODUCTION: The association between viral infections and pulmonary exacerbations in children with cystic fibrosis (cwCF) is well established. However, the question of whether cwCF are at a higher risk of COVID-19 or its adverse consequences remains controversial. METHODS: We conducted an observational, multicenter, cross-sectional study of cwCF infected by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) between March 2020 and June 2022, (first to sixth COVID-19 pandemic waves) in Spain. The study aimed to describe patients' basal characteristics, SARS-CoV-2 clinical manifestations and outcomes, and whether there were differences across the pandemic waves. RESULTS: During study time, 351 SARS-CoV2 infections were reported among 341 cwCF. Median age was 8.5 years (range 0-17) and 51% were female. Cases were unevenly distributed across the pandemic, with most cases (82%) clustered between November 2021 and June 2022 (sixth wave, also known as Omicron Wave due to the higher prevalence of this strain in that period in Spain). Most cwCF were asymptomatic (24.8%) or presented with mild Covid-19 symptoms (72.9%). Among symptomatic, most prevalent symptoms were fever (62%) and increased cough (53%). Infection occurring along the sixth wave was the only independent risk factor for being symptomatic. Just eight cwCF needed hospital admission. No multisystem inflammatory syndrome, persisting symptoms, long-term sequelae, or deaths were reported. CONCLUSIONS: Spanish current data indicate that cwCF do not experience higher risks of SARS-CoV-2 infection nor worse health outcomes or sequelae. Changes in patients' basal characteristics, clinical courses, and outcomes were detected across waves. While the pandemic continues, a worldwide monitoring of COVID-19 in pediatric CF patients is needed.


Assuntos
COVID-19 , Fibrose Cística , Humanos , Criança , Feminino , Recém-Nascido , Lactente , Pré-Escolar , Adolescente , Masculino , COVID-19/complicações , COVID-19/epidemiologia , SARS-CoV-2 , Estudos Transversais , Espanha/epidemiologia , Pandemias , Fibrose Cística/complicações , Fibrose Cística/epidemiologia , RNA Viral
11.
Biomed Res Int ; 2017: 9837508, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28758128

RESUMO

An anaphylactic shock is a time-critical emergency situation. The decision-making during emergencies is an important responsibility but difficult to study. Eye-tracking technology allows us to identify visual patterns involved in the decision-making. The aim of this pilot study was to evaluate two training models for the recognition and treatment of anaphylaxis by laypeople, based on expert assessment and eye-tracking technology. A cross-sectional quasi-experimental simulation study was made to evaluate the identification and treatment of anaphylaxis. 50 subjects were randomly assigned to four groups: three groups watching different training videos with content supervised by sanitary personnel and one control group who received face-to-face training during paediatric practice. To evaluate the learning, a simulation scenario represented by an anaphylaxis' victim was designed. A device capturing eye movement as well as expert valuation was used to evaluate the performance. The subjects that underwent paediatric face-to-face training achieved better and faster recognition of the anaphylaxis. They also used the adrenaline injector with better precision and less mistakes, and they needed a smaller number of visual fixations to recognise the anaphylaxis and to make the decision to inject epinephrine. Analysing the different video formats, mixed results were obtained. Therefore, they should be tested to evaluate their usability before implementation.


Assuntos
Anafilaxia/terapia , Aprendizagem , Educação de Pacientes como Assunto/métodos , Treinamento por Simulação/métodos , Adulto , Feminino , Humanos , Masculino
12.
J Med Genet ; 51(7): 475-8, 2014 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-24744435

RESUMO

BACKGROUND: Milroy and Milroy-like disease are rare disorders characterised by congenital lymphoedema caused by dysfunctional lymphatic vessel formation. Loss of extracellular response mediated by vascular endothelial growth factor receptor 3 (VEGFR-3) is associated with Milroy disease, and VEGFR-3 gene is mutated in around 70% of the cases diagnosed. The only genetic alteration known to be associated with Milroy-like disease was recently identified in a family with a frameshift mutation in vascular endothelial growth factor C (VEGFC) gene, which encodes a VEGFR3 ligand. METHODS AND RESULTS: We report a newborn patient with an external phenotype consistent with Milroy disease and a truncating mutation (p.R210X) in the VEGFC gene detected by exome sequence analysis. Subsequent analysis, by lymphoscintigraphic scan, performed for research purposes, allowed us to correct the diagnosis, confirming patient's disease as Milroy-like. The mutation segregates with the phenotype in the family according to a dominant model with full penetrance. CONCLUSIONS: The clinical presentation, similar to Milroy disease, indicates an overlapping of the external phenotype of both diseases, suggesting that genetic analysis of VEGFC would be useful in diagnosing patients that present with Milroy features but have no mutation in VEGFR-3. Establishing a well-defined genetic pattern would help with differential diagnosis.


Assuntos
Linfedema/diagnóstico , Fator C de Crescimento do Endotélio Vascular/genética , Códon de Terminação , Feminino , Estudos de Associação Genética , Predisposição Genética para Doença , Humanos , Lactente , Linfedema/genética , Linhagem
13.
Enferm. infecc. microbiol. clín. (Ed. impr.) ; 32(4): 246-249, abr. 2014. tab
Artigo em Espanhol | IBECS | ID: ibc-121556

RESUMO

INTRODUCCIÓN: La vacunación frente a rotavirus ha condicionado un descenso significativo de la enfermedad. El presente trabajo pretende evaluar las características clínicas y epidemiológicas de la gastroenteritis aguda (GEA) por virus en un área de alta cobertura vacunal frente a rotavirus. Método Evaluación prospectiva microbiológica mediante coprocultivo y reacción en cadena de la polimerasa en tiempo real (RT-PCR) para virus gastroentéricos, y genotipificado de las cepas de rotavirus de los casos de GEA en menores de 5 años que acudieron a urgencias o fueron hospitalizados en nuestro centro de noviembre a marzo de 2009-2010 y 2010-2011.ResultadosSe incluyeron 51 pacientes con una edad media (desviación estándar) de 19,1 (13,9) meses. El coprocultivo fue negativo en 23 muestras (45% de los casos), identificándose mediante RT-PCR un microorganismo causal en 16 de estas muestras (el 70%). El rotavirus fue el microorganismo más detectado (53%) y el genotipo G1[P8] el más abundante. En el 14% de los casos (7 pacientes) se identificó coinfección, siendo el rotavirus y el astrovirus los agentes más frecuentemente involucrados. Conclusiones El rotavirus, principalmente el G1[P8], se ha identificado como la causa más frecuente de GEA en nuestro estudio. La utilización de RT-PCR mejora significativamente la sensibilidad diagnóstica en el contexto de la GEA, y pone de relieve un porcentaje elevado de coinfecciones virales


INTRODUCTION: Vaccination against rotavirus has led to a significant decline of the disease. The aim of the present work is to evaluate the clinical and epidemiological features of the viral acute gastroenteritis(AGE) in an area with high immunization coverage against rotavirus. METHOD: A prospective microbiological evaluation was made of stool culture and Real Time Polymerase Chain Reaction (RT-PCR) to gastroenteric virus and genotyping of rotavirus strains in < 5 year-old with AGE episodes attended by or admitted to our hospital from November-March of 2009-2010 and 2010-2011.RESULTS: A total of 51 patients were included, with a mean age (standard deviation) of 19.1 (13.9) months. Stool culture was negative in 23 samples (45% of the samples analyzed), and it was identified a responsible microorganism in 70% by the RT-PCR (16 samples). Rotavirus was the most common isolated microorganism (53%), and G1[P8] the most frequent genotype. A co-infection was detected in 14% of samples(7 patients), and rotavirus and astrovirus were the most frequent etiological agents involved CONCLUSIONS: Rotavirus, basically G1[P8], is the most common AGE responsible agent identified in our study. The use of RT-PCR enhances the AGE diagnostic sensitivity, and uncovers an important number of viral co-infections


Assuntos
Humanos , Gastroenterite/microbiologia , Infecções por Rotavirus/microbiologia , Viroses/microbiologia , Rotavirus/isolamento & purificação , Vacinas contra Rotavirus/administração & dosagem , Técnicas de Genotipagem , Coinfecção/epidemiologia , Serviços de Vigilância Epidemiológica , Estudos Prospectivos
14.
Enferm Infecc Microbiol Clin ; 32(4): 246-9, 2014 Apr.
Artigo em Espanhol | MEDLINE | ID: mdl-24238660

RESUMO

INTRODUCTION: Vaccination against rotavirus has led to a significant decline of the disease. The aim of the present work is to evaluate the clinical and epidemiological features of the viral acute gastroenteritis (AGE) in an area with high immunization coverage against rotavirus. METHOD: A prospective microbiological evaluation was made of stool culture and Real Time Polymerase Chain Reaction (RT-PCR) to gastroenteric virus and genotyping of rotavirus strains in < 5 year-old with AGE episodes attended by or admitted to our hospital from November-March of 2009-2010 and 2010-2011. RESULTS: A total of 51 patients were included, with a mean age (standard deviation) of 19.1 (13.9) months. Stool culture was negative in 23 samples (45% of the samples analyzed), and it was identified a responsible microorganism in 70% by the RT-PCR (16 samples). Rotavirus was the most common isolated microorganism (53%), and G1[P8] the most frequent genotype. A co-infection was detected in 14% of samples (7 patients), and rotavirus and astrovirus were the most frequent etiological agents involved. CONCLUSIONS: Rotavirus, basically G1[P8], is the most common AGE responsible agent identified in our study. The use of RT-PCR enhances the AGE diagnostic sensitivity, and uncovers an important number of viral co-infections.


Assuntos
Gastroenterite/virologia , Infecções por Rotavirus/prevenção & controle , Vacinas contra Rotavirus , Doença Aguda , Feminino , Gastroenterite/diagnóstico , Gastroenterite/epidemiologia , Departamentos Hospitalares , Humanos , Lactente , Masculino , Pediatria , Estudos Prospectivos , Vacinação/estatística & dados numéricos
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